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Molecule
ID:133232
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₁₁FO₅
Molecular Mass
182.1469432
Exact Mass
182.05905167
Charge
0
InChI
InChI=1S/C6H11FO5/c7-3-5(10)4(9)2(1-8)12-6(3)11/h2-6,8-11H,1H2
InChIKey
ZCXUVYAZINUVJD-UHFFFAOYSA-N
Canonic Smiles
OCC1OC(O)C(C(C1O)O)F
Isomeric Smiles
C(C1C(C(C(C(O1)O)F)O)O)O
Calculated Properties
JChem
Acid pKa
11.021989
H Acceptors
5
H Donor
4
LogD (pH = 5.5)
-2.0414488
LogD (pH = 7.4)
-2.041551
Log P
-2.0414474
Molar Refractivity
34.2313
Polarizability
14.345064
Polar Surface Area
90.15
Rotatable Bonds
1
Lipinski's Rule of Five
true
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Data Source
Commercial Catalog
Sigma Aldrich
F5006
Academic Data
PubChem
315411
Names and Identifiers
Synonyms
FDG
2-Fluoro-2-deoxy-D-glucose
2-Deoxy-2-fluoro-D-glucose
IUPAC name
3-fluoro-6-(hydroxymethyl)oxane-2,4,5-triol
IUPAC Traditional name
2-deoxy-2-fluorohexopyranose
Registration numbers
MDL Number
MFCD00077527
PubChem SID
24894876
162227509
CAS Number
29702-43-0
PubChem CID
315411
Properties
Safety Information
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Source
European Hazard Symbols
Irritant (Xi)
Source
Storage Temperature
2-8°C
Source
Safety Statements
26
-
36
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
Risk Statements
36/37/38
Source
German water hazard class
3
Source
GHS Signal Word
Warning
Source
Product Information
Quality Level
PREMIUM
Source
Molecule Details
Sigma Aldrich
F5006
Biochem/physiol Actions
Glucose analog that inhibits cellular glycosylation. Natural isotope-form of 18F-FDG that can be taken up by cells but does not undergo metabolic glycolysis.
References
PubChem Literature
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Bioactivity
PubChem BioAssay